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https://ria.asturias.es/RIA/handle/123456789/7868
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Campo Dublin Core | Valor | Idioma |
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dc.contributor.author | Jiménez, Azucena | - |
dc.contributor.author | Pérez-Aguilar, M. Carmen | - |
dc.contributor.author | Cabal, María-Paz | - |
dc.contributor.author | Valdés, Carlos | - |
dc.date.accessioned | 2017-04-21T12:14:51Z | - |
dc.date.available | 2017-04-21T12:14:51Z | - |
dc.date.issued | 2016-02-02 | - |
dc.identifier.uri | https://ria.asturias.es/RIA/handle/123456789/7868 | - |
dc.description.abstract | 1,3-Diaryl-3-trifluoromethylcyclopropenes and 2-aryl- or 2-alkyl 1,3-diaryl-3-trifluoromethylcyclopropenes are prepared in a very simple way by reaction between 1,1,1-trifluoroacetophenone tosylhydrazones and terminal or internal alkynes respectively in a base promoted process that does not require the presence of any metal catalyst. The essential role of the trifluoromethyl group, which enables the formation of the cyclopropenes instead of the expected pyrazoles has been computationaly investigated,suggesting to the participacion of a free carbene. | eng |
dc.language.iso | eng | eng |
dc.relation.isreferencedby | No, esta versión no ha sido citada | eng |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/deed.es | eng |
dc.subject | Tosylhydrazone | eng |
dc.subject | Cyclopropene | eng |
dc.title | Synthesis of 1,3-Diaryl-3-trifluoromethylcyclopropenes by Transition-Metal-Free Reaction of 2,2,2-Trifluoroacetophenone Tosylhydrazones with Alkynes: The Effect of the Trifluoromethyl Group | eng |
dc.type | preprint | eng |
Aparece en las colecciones: | Open Access DRIVERset Química |
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